ongoing

Data indicate that patients with intracerebral hemorrhage (ICH) are at high risk for thromboembolic events and disability that is not being sufficiently mitigated by current treatment strategies. This is aggravated by the cessation of antithrombotic medications for significant periods after hemorrhage. These findings highlight the need for novel treatments that modify the high risk for major vascular events and functional outcomes in ICH survivors.

CoVasc-ICH 2 seeks to demonstrate that oral colchicine 0.5 mg daily is superior to placebo for improving the outcomes of ICH survivors with evidence or risk factors for atherosclerosis, when started within 72 hours from ICH onset. It follows the completion of the CoVasc-ICH pilot study (NCT05159219), where we were able to show feasibility of testing the use of low-dose colchicine in patients with acute ICH by recruiting a total of 100 participants across 11 research centres in Canada.

Study Type

Interventional - Drug

Study Design

Double-blind, randomized, placebo-controlled, phase III study

NO. of Countries

9

NO. of Sites

115

NO. of Participants

1125

Study Period

2025-2032

Sponsor

Population Health Research Institute

Canadian Institutes of Health Research (CIHR)

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